A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331564



Internal ID20864728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160027534..160037873hg38UCSC Ensembl
chr1:159997324..160007663hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg3810340
hg1910340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052438
Samples
Known GenesKCNJ10, PIGM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331564
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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