A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705427



Internal ID15095393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21821271..21864440hg38UCSC Ensembl
Innerchr1:22147764..22190933hg19UCSC Ensembl
Innerchr1:22020351..22063520hg18UCSC Ensembl
Innerchr1:21893070..21936239hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3843170
hg1943170
hg1843170
hg1743170
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515659
Supporting Variants
Samples
Known GenesHSPG2, LDLRAD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705427
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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