A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440742



Internal ID21098295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1576470..1577896hg38UCSC Ensembl
chr11:1597700..1599126hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381427
hg191427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989410
Samples
Known GenesKRTAP5-AS1, MOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440742
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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