A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998706



Internal ID19158242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:91426526..91737435hg38UCSC Ensembl
Innerchr2:91618895..91925461hg19UCSC Ensembl
Innerchr2:90982622..91289188hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg38310910
hg19306567
hg18306567
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3992n100
Supporting Variantsnssv3729113
Samples
Known GenesLOC654342
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998706
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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