A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694907



Internal ID15431559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:36900861..36902513hg38UCSC Ensembl
Innerchr4:36902483..36904135hg19UCSC Ensembl
Innerchr4:36578878..36580530hg18UCSC Ensembl
Innerchr4:36725049..36726701hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381653
hg191653
hg181653
hg171653
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522133
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694907
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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