A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173864



Internal ID15854375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26569931..26577491hg38UCSC Ensembl
Innerchr10:26858860..26866420hg19UCSC Ensembl
Innerchr10:26898866..26906426hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg387561
hg197561
hg187561
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550230
Supporting Variants
Samples1780862093_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173864
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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