A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667547



Internal ID15404199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149245608..149249548hg38UCSC Ensembl
Innerchr3:148963395..148967335hg19UCSC Ensembl
Innerchr3:150446085..150450025hg18UCSC Ensembl
Innerchr3:150446093..150450033hg17UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg383941
hg193941
hg183941
hg173941
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515663
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667547
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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