A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2758919



Internal ID17536933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80630938..80641673hg38UCSC Ensembl
Innerchr7:80260254..80270989hg19UCSC Ensembl
Innerchr7:80098190..80108925hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3810736
hg1910736
hg1810736
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv971195
Supporting Variants
SamplesHGDP01307
Known GenesCD36
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2758919
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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