A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516097



Internal ID15443390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:8949347..8951663hg38UCSC Ensembl
Innerchr1:9009406..9011722hg19UCSC Ensembl
Innerchr1:8931993..8934309hg18UCSC Ensembl
Innerchr1:8943672..8945988hg17UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg382317
hg192317
hg182317
hg172317
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv666175, nssv660321, nssv671923, nssv671111, nssv669183, nssv660728, nssv692368, nssv660579, nssv671439
Samples
Known GenesCA6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516097
Frequency
Sample Size2026
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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