A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653789



Internal ID15390441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:153748053..153750016hg38UCSC Ensembl
Innerchr3:153465842..153467805hg19UCSC Ensembl
Innerchr3:154948532..154950495hg18UCSC Ensembl
Innerchr3:154948540..154950503hg17UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg381964
hg191964
hg181964
hg171964
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517101
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653789
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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