A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705358



Internal ID15095324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:88680820..88692916hg38UCSC Ensembl
Innerchr5:87976637..87988733hg19UCSC Ensembl
Innerchr5:88012393..88024489hg18UCSC Ensembl
Innerchr5:88012393..88024489hg17UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3812097
hg1912097
hg1812097
hg1712097
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515977
Supporting Variants
Samples
Known GenesLINC00461
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705358
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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