A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001873



Internal ID19091090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:175967297..176023275hg38UCSC Ensembl
Innerchr2:176832025..176888003hg19UCSC Ensembl
Innerchr2:176540271..176596249hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3855979
hg1955979
hg1855979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3583040
Samples
Known GenesKIAA1715
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001873
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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