A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv736776



Internal ID16030732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:210549210..210550669hg38UCSC Ensembl
Innerchr1:210722554..210724013hg19UCSC Ensembl
Innerchr1:208789177..208790636hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg381460
hg191460
hg181460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549111
Supporting Variants
Samples
Known GenesHHAT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv736776
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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