A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056753



Internal ID19145972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:37472812..37525041hg38UCSC Ensembl
Innerchr19:37963714..38015943hg19UCSC Ensembl
Innerchr19:42655554..42707783hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3852230
hg1952230
hg1852230
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568191, nssv3568190
Samples
Known GenesZNF570, ZNF793
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056753
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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