A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7171n223



Internal ID22810139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149945314..154240405hg38UCSC Ensembl
chr7:149642403..153937490hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg384295092
hg194295088
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6566842, nsv6572121, nsv6572365, nsv6555662, nsv6575198, nsv6557258, nsv6568265, nsv6563000, nsv6559523, nsv6572091, nsv6561525, nsv6572326, nsv6566056
Samples
Known GenesABCB8, ABCF2, ACTR3B, ACTR3C, AGAP3, AOC1, ASB10, ASIC3, ATG9B, CDK5, CHPF2, CRYGN, DPP6, FABP5P3, FASTK, GALNT11, GALNTL5, GBX1, GIMAP1, GIMAP1-GIMAP5, GIMAP2, GIMAP4, GIMAP5, GIMAP6, GIMAP7, GIMAP8, KCNH2, KMT2C, LINC00996, LINC01003, LOC728743, LRRC61, MIR3907, MIR671, NOS3, NUB1, PRKAG2, PRKAG2-AS1, RARRES2, REPIN1, RHEB, RNU6-33P, RNU6-34P, SLC4A2, SMARCD3, TMEM176A, TMEM176B, TMUB1, WDR86, WDR86-AS1, XRCC2, ZBED6CL, ZNF775
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7171n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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