A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007304



Internal ID18749835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16886207..16935740hg38UCSC Ensembl
Innerchr1:17212702..17262235hg19UCSC Ensembl
Innerchr1:17085289..17134822hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3849534
hg1949534
hg1849534
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv117n100
Supporting Variantsnssv3462833, nssv3474193
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)nsv1007304
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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