A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519592



Internal ID15446885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:43555801..43558623hg38UCSC Ensembl
Innerchr7:43595400..43598222hg19UCSC Ensembl
Innerchr7:43561925..43564747hg18UCSC Ensembl
Innerchr7:43368640..43371462hg17UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg382823
hg192823
hg182823
hg172823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696940
Samples
Known GenesHECW1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519592
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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