A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021269



Internal ID19110486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:139020930..139083262hg38UCSC Ensembl
Innerchr7:138705676..138768008hg19UCSC Ensembl
Innerchr7:138356216..138418548hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3862333
hg1962333
hg1862333
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6640n100
Supporting Variantsnssv3664244
Samples
Known GenesZC3HAV1, ZC3HAV1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021269
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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