A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016826



Internal ID19106043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:98296821..98334405hg38UCSC Ensembl
Innerchr7:97926133..97963717hg19UCSC Ensembl
Innerchr7:97764069..97801653hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3837585
hg1937585
hg1837585
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655295, nssv3655296
Samples
Known GenesBAIAP2L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016826
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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