A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153929



Internal ID15853815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:51981695..52079679hg38UCSC Ensembl
Innerchr5:51277529..51375513hg19UCSC Ensembl
Innerchr5:51313286..51411270hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3897985
hg1997985
hg1897985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598147
Supporting Variants
Samples1780854449_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153929
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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