A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552201



Internal ID16339610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:113904402..113934873hg38UCSC Ensembl
Innerchr10:115664161..115694632hg19UCSC Ensembl
Innerchr10:115654151..115684622hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3830472
hg1930472
hg1830472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv758782
Samples
Known GenesNHLRC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552201
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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