A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065985



Internal ID18808516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:2902148..2963345hg38UCSC Ensembl
Innerchr19:2902146..2963343hg19UCSC Ensembl
Innerchr19:2853146..2914343hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3861198
hg1961198
hg1861198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564605
Samples
Known GenesZNF57, ZNF77
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065985
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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