A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331652



Internal ID20864817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:71097110..71097801hg38UCSC Ensembl
chr1:71562793..71563484hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38692
hg19692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062858
Samples
Known GenesZRANB2-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331652
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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