A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3231688



Internal ID22372301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:35603726..35610862hg38UCSC Ensembl
Outerchr10:35892654..35899790hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg381837
hg191837
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14283625, nssv14283622, nssv14283621, nssv14283619, nssv14283626, nssv14283624, nssv14283623, nssv14283620, nssv14283618
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesGJD4
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3231688
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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