A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv675994



Internal ID15065960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:87974428..87976303hg38UCSC Ensembl
Innerchr7:87603743..87605618hg19UCSC Ensembl
Innerchr7:87441679..87443554hg18UCSC Ensembl
Innerchr7:87248394..87250269hg17UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg381876
hg191876
hg181876
hg171876
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517676
Supporting Variants
Samples
Known GenesADAM22
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv675994
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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