A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001771



Internal ID19090988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:57371417..57602503hg38UCSC Ensembl
Innerchr1:57837089..58068175hg19UCSC Ensembl
Innerchr1:57609677..57840763hg18UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38231087
hg19231087
hg18231087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3481127
Samples
Known GenesDAB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001771
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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