A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702825



Internal ID15439477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:95164366..95168109hg38UCSC Ensembl
Innerchr12:95558142..95561885hg19UCSC Ensembl
Innerchr12:94082273..94086016hg18UCSC Ensembl
Innerchr12:94060610..94064353hg17UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg383744
hg193744
hg183744
hg173744
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526515
Supporting Variants
Samples
Known GenesFGD6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702825
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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