A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657045



Internal ID15047011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42817913..43158934hg38UCSC Ensembl
Innerchr19:43322065..43663086hg19UCSC Ensembl
Innerchr19:48013905..48354926hg18UCSC Ensembl
Innerchr19:48013905..48354926hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38341022
hg19341022
hg18341022
hg17341022
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516973
Supporting Variants
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG2, PSG6, PSG7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657045
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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