A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517676



Internal ID15098283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:87974428..87976931hg38UCSC Ensembl
Innerchr7:87603743..87606246hg19UCSC Ensembl
Innerchr7:87441679..87444182hg18UCSC Ensembl
Innerchr7:87248394..87250897hg17UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg382504
hg192504
hg182504
hg172504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv683500, nssv680205, nssv675683, nssv663311, nssv675994, nssv683153, nssv662368, nssv652791, nssv663820, nssv670129
Samples
Known GenesADAM22
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517676
Frequency
Sample Size2026
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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