A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705602



Internal ID15095568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:124529851..124542912hg38UCSC Ensembl
Innerchr10:126218420..126231481hg19UCSC Ensembl
Innerchr10:126208410..126221471hg18UCSC Ensembl
Innerchr10:126208410..126221471hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3813062
hg1913062
hg1813062
hg1713062
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521161
Supporting Variants
Samples
Known GenesLHPP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705602
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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