A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997712



Internal ID18810562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16617106..16643493hg38UCSC Ensembl
Innerchr1:16943601..16969988hg19UCSC Ensembl
Innerchr1:16816188..16842575hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3826388
hg1926388
hg1826388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv69n100
Supporting Variantsnssv3464370
Samples
Known GenesCROCCP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997712
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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