A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032777



Internal ID19121999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:91609436..91643084hg38UCSC Ensembl
Innerchr6:92319154..92352802hg19UCSC Ensembl
Innerchr6:92375875..92409523hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3833649
hg1933649
hg1833649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648963
Samples
Known GenesCASC6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032777
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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