A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2762358



Internal ID17528836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74354204..74370569hg38UCSC Ensembl
Innerchr10:76113962..76130327hg19UCSC Ensembl
Innerchr10:75783968..75800333hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3816366
hg1916366
hg1816366
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv971906
Supporting Variants
SamplesHGDP01284
Known GenesADK
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2762358
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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