A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350590



Internal ID21008143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218309039..218369142hg38UCSC Ensembl
chr2:219173762..219233865hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3860104
hg1960104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085886
Samples
Known GenesC2orf62, MIR6810, PNKD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350590
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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