A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319082



Internal ID20852174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77154884..77155407hg38UCSC Ensembl
chr1:77620569..77621092hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063197
Samples
Known GenesPIGK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319082
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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