A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1077607



Internal ID15930793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:139113..177753hg38UCSC Ensembl
Innerchr7:139113..177753hg19UCSC Ensembl
Innerchr7:234196..272836hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3838641
hg1938641
hg1838641
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605599
Supporting Variants
Samples
Known GenesLOC100507642
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1077607
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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