A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334311



Internal ID20867495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7642949..7643210hg38UCSC Ensembl
chr1:7703009..7703270hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063127
Samples
Known GenesCAMTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334311
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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