A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684557



Internal ID15074523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:37491775..37509678hg38UCSC Ensembl
Innerchr1:37957376..37975279hg19UCSC Ensembl
Innerchr1:37729963..37747866hg18UCSC Ensembl
Innerchr1:37626469..37644372hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3817904
hg1917904
hg1817904
hg1717904
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519551
Supporting Variants
Samples
Known GenesMEAF6, MIR5581
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv684557
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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