A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579986



Internal ID18878267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:97107032..97545714hg38UCSC Ensembl
Innerchr2:97772769..98162177hg19UCSC Ensembl
Innerchr2:97136496..97528609hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38438683
hg19389409
hg18392114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004521
Supporting Variants
Samples
Known GenesANKRD36, ANKRD36B, LOC100506076, LOC100506123
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3579986
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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