A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275183



Internal ID20842223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146996771..152901398hg38UCSC Ensembl
chr7:146693863..152598483hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg385904628
hg195904621
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558115
Supporting Variants
Samples
Known GenesABCB8, ABCF2, ACTR3B, ACTR3C, AGAP3, AOC1, ASB10, ASIC3, ATG9B, ATP6V0E2, ATP6V0E2-AS1, C7orf33, CDK5, CHPF2, CNTNAP2, CRYGN, CUL1, EZH2, FABP5P3, FASTK, GALNT11, GALNTL5, GBX1, GIMAP1, GIMAP1-GIMAP5, GIMAP2, GIMAP4, GIMAP5, GIMAP6, GIMAP7, GIMAP8, KCNH2, KMT2C, KRBA1, LINC00996, LINC01003, LOC155060, LOC728743, LRRC61, MIR3907, MIR548F3, MIR548F4, MIR548I4, MIR548T, MIR671, NOS3, NUB1, PDIA4, PRKAG2, PRKAG2-AS1, RARRES2, REPIN1, RHEB, RNU6-33P, RNU6-34P, SLC4A2, SMARCD3, SSPO, TMEM176A, TMEM176B, TMUB1, WDR86, WDR86-AS1, XRCC2, ZBED6CL, ZNF212, ZNF282, ZNF398, ZNF425, ZNF467, ZNF746, ZNF767, ZNF775, ZNF777, ZNF783, ZNF786, ZNF862
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275183
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer