A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348840



Internal ID21006393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:7432400..7433032hg38UCSC Ensembl
chr2:7572531..7573163hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090210
Samples
Known GenesLOC100506274
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348840
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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