A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705311



Internal ID15441963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:56583288..56593898hg38UCSC Ensembl
Innerchr1:57048961..57059571hg19UCSC Ensembl
Innerchr1:56821549..56832159hg18UCSC Ensembl
Innerchr1:56760982..56771592hg17UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3810611
hg1910611
hg1810611
hg1710611
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528673
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705311
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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