A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567722



Internal ID18519317
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 StatusS
Merged Variantsnsv1062376
Supporting Variants
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)nssv3567722
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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