A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604158



Internal ID20977229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71396004..71967385hg38UCSC Ensembl
chr7:70860990..71432370hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38571382
hg19571381
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230220
Samples
Known GenesCALN1, WBSCR17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604158
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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