A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604844



Internal ID20977915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35869556..35870016hg38UCSC Ensembl
chr7:35909166..35909626hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg38461
hg19461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153708
Samples
Known GenesSEPT7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604844
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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