A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2765894



Internal ID17789830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:145450009..145457581hg38UCSC Ensembl
Innerchr7:145147102..145154674hg19UCSC Ensembl
Innerchr7:144778035..144785607hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg387573
hg197573
hg187573
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv971555
Supporting Variants
SamplesHGDP00665
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2765894
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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