A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609797



Internal ID20982868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:56663744..56664305hg38UCSC Ensembl
chr7:56731437..56731998hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38562
hg19562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157203
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609797
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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