A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527623



Internal ID22397010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105909607..105909663hg38UCSC Ensembl
chr6:106357482..106357538hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14330692, nssv14330690, nssv14330689, nssv14330691, nssv14330686, nssv14330688, nssv14330687
SamplesHG00512, NA19239, HG00731, HG00732, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527623
Frequency
Sample Size9
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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