A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572365



Internal ID20945436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:150750106..154240405hg38UCSC Ensembl
chr7:150447194..153937490hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg383490300
hg193490297
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7171n223
Supporting Variantsnssv18273078
Samples
Known GenesABCB8, ABCF2, ACTR3B, AGAP3, AOC1, ASB10, ASIC3, ATG9B, CDK5, CHPF2, CRYGN, DPP6, FABP5P3, FASTK, GALNT11, GALNTL5, GBX1, KCNH2, KMT2C, LINC01003, MIR3907, MIR671, NOS3, NUB1, PRKAG2, PRKAG2-AS1, RHEB, SLC4A2, SMARCD3, TMEM176A, TMEM176B, TMUB1, WDR86, WDR86-AS1, XRCC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572365
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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