A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034256



Internal ID19123478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:113382365..113472588hg38UCSC Ensembl
Innerchr6:113703567..113793790hg19UCSC Ensembl
Innerchr6:113810260..113900483hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3890224
hg1990224
hg1890224
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6138n100
Supporting Variantsnssv3654305
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034256
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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