A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549929



Internal ID16337338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6635805..6803275hg38UCSC Ensembl
Innerchr10:6677767..6845237hg19UCSC Ensembl
Innerchr10:6717773..6885243hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38167471
hg19167471
hg18167471
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv743555, nssv743554
Samples
Known GenesLINC00706, LINC00707
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549929
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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