A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701451



Internal ID15438103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:121461679..121466508hg38UCSC Ensembl
Innerchr4:122382834..122387663hg19UCSC Ensembl
Innerchr4:122602284..122607113hg18UCSC Ensembl
Innerchr4:122740439..122745268hg17UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg384830
hg194830
hg184830
hg174830
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516606
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701451
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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