A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021077



Internal ID19110295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:11874472..11920836hg38UCSC Ensembl
Innerchr7:11914098..11960462hg19UCSC Ensembl
Innerchr7:11880623..11926987hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3846365
hg1946365
hg1846365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3642952
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021077
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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