A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703441



Internal ID15093407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185483851..185498735hg38UCSC Ensembl
Innerchr4:186405005..186419889hg19UCSC Ensembl
Innerchr4:186641999..186656883hg18UCSC Ensembl
Innerchr4:186780154..186795038hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3814885
hg1914885
hg1814885
hg1714885
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517035
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703441
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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