A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056970



Internal ID19146189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6788869..6835645hg38UCSC Ensembl
Innerchr19:6788880..6835656hg19UCSC Ensembl
Innerchr19:6739880..6786656hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3846777
hg1946777
hg1846777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564615
Samples
Known GenesVAV1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056970
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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