A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347175



Internal ID21004728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:71086552..71090701hg38UCSC Ensembl
chr2:71313682..71317831hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg384150
hg194150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089587
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347175
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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