A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317077



Internal ID20850161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7605016..7609014hg38UCSC Ensembl
chr1:7665076..7669074hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg383999
hg193999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064083
Samples
Known GenesCAMTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317077
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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