A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703439



Internal ID15440091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:84869357..84895424hg38UCSC Ensembl
Innerchr2:85096481..85122548hg19UCSC Ensembl
Innerchr2:84949992..84976059hg18UCSC Ensembl
Innerchr2:85008139..85034206hg17UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3826068
hg1926068
hg1826068
hg1726068
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527061
Supporting Variants
Samples
Known GenesTRABD2A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703439
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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