A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604996



Internal ID16045719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:159931465..159977298hg38UCSC Ensembl
Innerchr6:160352497..160398330hg19UCSC Ensembl
Innerchr6:160272487..160318320hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3845834
hg1945834
hg1845834
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1075168
Samples
Known GenesIGF2R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604996
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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