A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv736783



Internal ID16030739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:210549210..210551373hg38UCSC Ensembl
Innerchr1:210722554..210724717hg19UCSC Ensembl
Innerchr1:208789177..208791340hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg382164
hg192164
hg182164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549114
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)nssv736783
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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