A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3708241



Internal ID18659836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:8249238..8451181hg38UCSC Ensembl
Innerchr12:8401834..8603777hg19UCSC Ensembl
Innerchr12:8293101..8495044hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38201944
hg19201944
hg18201944
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046231
Supporting Variants
Samples
Known GenesLINC00937
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3708241
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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