A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1058386



Internal ID15564886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:36983434..37010969hg38UCSC Ensembl
Innerchr6:36951210..36978745hg19UCSC Ensembl
Innerchr6:37059188..37086723hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3827536
hg1927536
hg1827536
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602952
Supporting Variants
Samples
Known GenesFGD2, MTCH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1058386
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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