A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012684



Internal ID19101901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16909177..16935740hg38UCSC Ensembl
Innerchr1:17235672..17262235hg19UCSC Ensembl
Innerchr1:17108259..17134822hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3826564
hg1926564
hg1826564
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv124n100
Supporting Variantsnssv3700271, nssv3700272, nssv3480343, nssv3700270, nssv3478193
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)nsv1012684
Frequency
Sample Size11257
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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