A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602921



Internal ID20975992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32574325..32609980hg38UCSC Ensembl
chr7:32613937..32649592hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3835656
hg1935656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156119
Samples
Known GenesAVL9, DPY19L1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602921
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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