A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705660



Internal ID15095626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143917935..143937036hg38UCSC Ensembl
Innerchr8:144992103..145011204hg19UCSC Ensembl
Innerchr8:145064091..145083192hg18UCSC Ensembl
Innerchr8:145064091..145083192hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3819102
hg1919102
hg1819102
hg1719102
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515809
Supporting Variants
Samples
Known GenesPLEC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705660
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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