A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002932



Internal ID18745464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16888315..16931063hg38UCSC Ensembl
Innerchr1:17214810..17257558hg19UCSC Ensembl
Innerchr1:17087397..17130145hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3842749
hg1942749
hg1842749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv115n100
Supporting Variantsnssv3468311
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)nsv1002932
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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