A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032157



Internal ID18774691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:36591870..36627946hg38UCSC Ensembl
Innerchr7:36631476..36667552hg19UCSC Ensembl
Innerchr7:36598001..36634077hg18UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3836077
hg1936077
hg1836077
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643424
Samples
Known GenesAOAH, AOAH-IT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032157
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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