A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059162



Internal ID18801693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:75895450..76696919hg38UCSC Ensembl
Innerchr16:75929348..76730816hg19UCSC Ensembl
Innerchr16:74486849..75288317hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38801470
hg19801469
hg18801469
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559631
Samples
Known GenesCNTNAP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059162
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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