A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601979



Internal ID20975050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:85047939..85048551hg38UCSC Ensembl
chr7:84677255..84677867hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38613
hg19613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161132
Samples
Known GenesSEMA3D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601979
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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