A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003988



Internal ID18746519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16876990..16934756hg38UCSC Ensembl
Innerchr1:17203485..17261251hg19UCSC Ensembl
Innerchr1:17076072..17133838hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3857767
hg1957767
hg1857767
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv113n100
Supporting Variantsnssv3700213
Samples
Known GenesCROCC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003988
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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