A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062376



Internal ID18804907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:61077849..61126693hg38UCSC Ensembl
Innerchr17:59155210..59204054hg19UCSC Ensembl
Innerchr17:56509992..56558836hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3848845
hg1948845
hg1848845
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567722
Samples
Known GenesBCAS3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062376
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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