A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527692



Internal ID15454985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:27660023..27660487hg38UCSC Ensembl
Innerchr4:27661645..27662109hg19UCSC Ensembl
Innerchr4:27270743..27271207hg18UCSC Ensembl
Innerchr4:27337914..27338378hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38465
hg19465
hg18465
hg17465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704168
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527692
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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