A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002717



Internal ID18745249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16884145..16935740hg38UCSC Ensembl
Innerchr1:17210640..17262235hg19UCSC Ensembl
Innerchr1:17083227..17134822hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3851596
hg1951596
hg1851596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv115n100
Supporting Variantsnssv3700260, nssv3468153, nssv3473068
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)nsv1002717
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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