A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3492380



Internal ID19080021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:210431390..210441937hg38UCSC Ensembl
Innerchr1:210604734..210615281hg19UCSC Ensembl
Innerchr1:208671357..208681904hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3810548
hg1910548
hg1810548
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001747
Supporting Variants
Samples
Known GenesHHAT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3492380
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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