A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525345



Internal ID15452638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:141208160..141211808hg38UCSC Ensembl
Innerchr4:142129314..142132962hg19UCSC Ensembl
Innerchr4:142348764..142352412hg18UCSC Ensembl
Innerchr4:142486919..142490567hg17UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg383649
hg193649
hg183649
hg173649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701463
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525345
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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