A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1094836



Internal ID15948022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140175821..140176843hg38UCSC Ensembl
Innerchr7:139875621..139876643hg19UCSC Ensembl
Innerchr7:139522090..139523112hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381023
hg191023
hg181023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608491
Supporting Variants
Samples
Known GenesKDM7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1094836
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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